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OpenTrials
Completed

NCT Number: NCT01846637

Two or Five cm From Pylorus During Laparoscopic Sleeve Gastrectomy

The investigators compare two techniques for laparoscopic sleeve gastrectomy. in the first one the distal margin of stapling is 2 cm from the pylorus and in the second it is 6 cm away from the pylorus.

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Key information

Conditions

Morbid Obesity Body Weight Nutrition Disorders Nutritional and Metabolic Diseases Obesity Obesity, Morbid Overnutrition Overweight Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gastroenterology Surgical Center

Al Mansurah, Dakahlia Governorate, 35516, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • morbid obese patients

Exclusion criteria

  • contraindication to laparoscopy

Treatment and study plan

Laparoscopic sleeve gastrectomy

Procedure

Primary outcomes

  1. percentage of excess weight loss

    Time frame: 2 years

Secondary outcomes

  1. complications

    Time frame: 2 years

Other outcomes

  1. improvement of comorbidities

    Time frame: 2 years

Interested in participating?

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Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Comparative Study Between Two and Five cm Resection During Laparoscopic Sleeve Gastrectomy

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
May 3, 2013
Registry last updated
May 6, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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